The cloning of plant E2F, a retinoblastoma-binding protein, reveals uniqueand conserved features with animal G(1)/S regulators

Citation
E. Ramirez-parra et al., The cloning of plant E2F, a retinoblastoma-binding protein, reveals uniqueand conserved features with animal G(1)/S regulators, NUCL ACID R, 27(17), 1999, pp. 3527-3533
Citations number
54
Categorie Soggetti
Biochemistry & Biophysics
Journal title
NUCLEIC ACIDS RESEARCH
ISSN journal
03051048 → ACNP
Volume
27
Issue
17
Year of publication
1999
Pages
3527 - 3533
Database
ISI
SICI code
0305-1048(19990901)27:17<3527:TCOPEA>2.0.ZU;2-M
Abstract
Association of the retinoblastoma (Rb) protein with E2F transcription facto rs is central to cell cycle-specific gene expression and growth in animal c ells, Whether Rb-E2F complexes are also involved in plant cell growth and d ifferentiation is still unknown since E2F proteins have not yet been identi fied in plants, Here we report the isolation and characterisation of a whea t E2F (TmE2F) cDNA clone. Interestingly, the overall domain organisation of plant E2F is related to the human E2F-1/2/3 subset but its primary sequenc e is slightly more related to the E2F-4/5 subset, TmE2F-Rb binding depends on residues, located at the C-terminus, which are different from those of a nimal E2Fs, However, the acidic or hydrophobic nature of certain residues i s maintained, strongly suggesting that they may have a crucial role in E2F activities. Plant E2F is expressed in proliferating cultured cells and in d ifferentiated tissues and is up-regulated early in S phase, Our studies rei nforce the idea that G(1)/S regulators in plants are unrelated to those of yeast cells but similar to those of animal cells and provide new tools to a nalyse the links between cell cycle regulators, plant growth and developmen tal signals.